Chemist jobs in Boulder, CO

Analytical Chemist Department: Quality Employment Type: Full-Time Compensation: $75,00-$100,000 VPI is a leader in high-quality, specialized pharmaceutical compounding, dedicated to patient safety and therapeutic efficacy. We empower healthcare professionals with innovative, customized medications that meet unique patient needs. This role is essential to our mission, ensuring every product released meets the highest standards of quality and compliance. VPI Compounding is seeking a highly skilled and meticulous Analytical Chemist to join our dedicated Quality team. This critical role is responsible for the integrity, safety, and efficacy of our compounded pharmaceutical products. The successful candidate will perform chemical analyses, lead method development, and drive compliance with rigorous regulatory standards, serving as a pillar of our commitment to quality. Key Responsibilities: Chemical Analysis & Quality Assurance Execute complex qualitative and quantitative analysis of raw materials, in-process samples, and finished pharmaceutical products. Expertly operate, troubleshoot, and maintain advanced analytical instrumentation, including High-Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS), and UV/Vis spectrophotometry. Method Development & Validation Design, develop, and rigorously validate new analytical testing methods for novel and existing pharmaceutical compounds. Strategically optimize existing testing procedures to significantly enhance laboratory throughput, accuracy, and efficiency. Regulatory Compliance & Documentation Implement and strictly uphold quality control procedures in full compliance with FDA regulations, cGMP guidelines, and all internal Standard Operating Procedures (SOPs). Prepare comprehensive, detailed reports and documentation packages necessary to support regulatory submissions and internal quality audits. Collaboration & Innovation Serve as the key analytical partner to the Formulation Team, providing data-driven insights to support product consistency and innovation. Maintain a current understanding of advancements in analytical techniques and pharmaceutical compounding to continuously elevate laboratory practices. Qualifications: Education & Experience: Required: Bachelors degree in Chemistry, Analytical Chemistry, or a closely related scientific field. (Masters or PhD highly preferred) Minimum of 2 years of hands-on experience in an analytical chemistry laboratory, preferably within a pharmaceutical, regulated, or compounding environment. Proven technical expertise operating and maintaining advanced chromatographic and spectroscopic equipment. Skills & Attributes: Exceptional attention to detail and ability to execute complex procedures accurately. Strong verbal and written communication skills to effectively report technical data and findings. Demonstrated problem-solving abilities in a laboratory setting. Physical Requirements: Ability to perform fine motor movements necessary for laboratory work. Must be able to work at a computer workstation for extended periods. Benefits: Company-paid health, dental, and vision insurance (Premiums covered by VPI) 401(k) with employer match Paid Holidays, Floating Holidays, and PTO Tuition and Certification Reimbursement RTD EcoPass for public transportation Opportunities for professional growth and development Equal Opportunity Employer: VPI Compounding Pharmacy is an Equal Employment Opportunity (EEO) employer. We are committed to providing equal opportunity for all qualified persons employed by or seeking employment with VPI, regardless of race, color, creed, religion, sex, sexual preference, national origin, age, marital status, veteran status, or non-job related handicaps. This policy extends to all areas of employment, including recruitment, job assignment, promotion, and other terms of employment.

Imagine yourself… * Doing meaningful work that makes an everyday impact on the world around you. * Growing your expertise and expanding your skillset with every project. * Contributing to a brighter, more sustainable future. At Hach (************** a Veralto company, we ensure water quality for people around the world, and every associate plays a vital role in that mission. Our founding vision is to make water analysis better-faster, simpler, greener, and more informative. We accomplish this through teamwork, customer partnerships, passionate experts, and reliable, easy-to-use solutions. As part of our team, you'll make an immediate, measurable impact on a global scale by enabling the world's everyday water needs. You'll join a respectful and collaborative community that fosters career growth and professional development, supported by resources that help you thrive. At Hach, we value your authenticity and want your talents to shine. Motivated by the highest possible stakes in climate change and global health, we're innovating within a rapidly digitizing industry to develop technologies that safeguard our water and protect the environment. More about us: ***************************** We offer: * Paid time off * Professional onboarding and training opportunities * Career coaching and development opportunities * Health, dental, vision benefits * 401(k) * A supportive, passionate team environment POSITION SUMMARY Reporting to the Manager, Chemistry, the Chemist II works as part of a small team of chemists and cross-functional partners to research, develop, design, modify, test, and prepare chemical products and product applications. This role plays a key part in solving complex chemical challenges, developing new analytical methods for Hach's instrumentation, and supporting the manufacturing and operationalization of chemical products. The R&D Chemist II brings a continuous improvement mindset, works with minimal supervision, and utilizes Hach's systems and expertise to drive innovation in water analysis. This position is part of the R&D Chemistry Department located in Loveland, CO and will be on-site. In this role, a typical day will look like: * Driving and maintaining safe working environments. * Developing new chemical methods of analysis through independent research. * Demonstrating a wide range of analytical techniques, methods, chemical principles, and laboratory practices. * Creating formularies and quality control procedures for new and modified test reagents. * Working closely with operations teams to evaluate and implement manufacturing processes. * Reviewing technical journals and competitive literature to maintain technological competitiveness. * Collaborating with cross-functional groups on project planning, brainstorming, and problem-solving. * Providing chemistry expertise to project teams or business units. * Supporting customers or service teams with analysis-related questions. * Reviewing reports for technical accuracy and adherence to quality systems. * Writing chemical analysis procedures for product formularies and controls. * Recommending improvements to procedures, safety measures, or departmental performance. The essential requirements of the job include: * Bachelor's degree in Chemistry or related field + 3 years industrial experience, OR a Master's degree in Chemistry. * Research experience outside of academic coursework. * Demonstrated knowledge in at least two areas of chemistry (e.g., analytical, organic, inorganic). * Proven ability in chemical design, characterization, functional testing, and problem-solving. * Ability to communicate and present technical information clearly to both technical and non-technical audiences. Preferred Qualifications: * Hands-on experience in formulary development. * Hands-on experience in electrochemical techniques. About Veralto Hach is proud to be part of the Water Quality segment of Veralto (NYSE: VLTO), a $5B global leader dedicated to ensuring access to clean water, safe food and medicine, and trusted essential goods. When you join Veralto's global network of 17,000 associates, you join a culture where purpose meets possibility-where your work has everyday impact on the essentials the world relies on, and where your career can grow through world-class development. Together, we're Safeguarding the World's Most Vital Resources - and building rewarding careers along the way. US ONLY: The below range reflects the range of possible compensation for this role at the time of this posting. We may ultimately pay more or less than the posted range. This range may be modified in the future. An associate's position within the salary range will be based on several factors, including, but not limited to, relevant education, qualifications, certifications, experience, skills, seniority, geographic location, performance, shift, travel requirements, sales or revenue-based metrics, any collective bargaining agreements, and business or organizational needs. The compensation range for this role is $68,000 - $75,000 USD per year. This job is also eligible for Bonus Pay. We offer a comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. US residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Veralto Corporation and all Veralto Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@veralto.com to request accommodation. Unsolicited Assistance We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at any of the Veralto companies, in any form without a valid, signed search agreement in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Veralto and its companies. No fee will be paid in the event the candidate is hired by Veralto and its companies because of the unsolicited referral.

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical, and biotech companies manufacture medicines with the ultimate goal of improving people's lives. Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being. Our People VisionWe strive for excellence. We share our passion. Together, we make a difference in patients' lives. SUMMARY Acts to drive and demonstrate the technology for the planning and execution of development and implementation of chemical processes. Ensures that the chemistry is sufficient to meet goals on process yields, throughputs, and QSHE requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned: Familiarity with general TFF/ultra filtration setup, operation, and components Experience with lab and/or mid-large scale TFF/ultra filtration processing Knowledge of various types of TFF filtration methods and systems Understanding of key operating/scalable parameters for TFF/ultra filtration and ability to determine such parameters during process familiarization/optimization Provides technical support to lab or plant processes Works effectively in a team-oriented environment Presents work orally and in form of written development reports Adheres to GDP and SOPs in all aspects of work Independently plans and executes experiments, while working in a project team, toward development of viable commercial processes Demonstrates a clear understanding of technical issues and the requirements of a viable manufacturing process Executes procedures, processes, and methods for solutions to chemical and technical problems on a lab or plant scale Ensures that the chemistry is capable of meeting cost, yield, throughput, and QSHE goals on assigned processes Leads a team to accomplish the development, transfer, or implementation of technology at a lab or plant scale Develops and supports scalable processes and provides technical expertise and support during lab or plant operations LEADERSHIP & BUDGET RESPONSIBILITIES Demonstrates a positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons. This position has no supervisory responsibilities. Provides technical expertise to manufacturing. SAFETY & ENVIRONMENTAL RESPONSIBILITIES Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience. QUALITY RESPONSIBILITIES Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC's Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company. cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelor's Degree (BS) in Organic Chemistry and 5 years related experience and/or training; or equivalent combination of education and experience. TFF/Untra filtration experience is required; and Peptide and GMP experience is a plus. LANGUAGE SKILLS Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to develop bench scale laboratory procedures into step-by-step operating instructions for chemical operators. Ability to effectively present information to top management, public groups, and/or boards of directors. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. REASONING ABILITY Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables. Ability to apply scientific methods to experimentally prove cause and effect. CERTIFICATES, LICENSES, REGISTRATIONS Domestic and international travel required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The noise level in the work environment is usually moderate. CORE COMPETENCIES These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity. Demonstrates a positive attitude Strong background in chemistry or a related scientific field Working knowledge of regulatory issues in Pharmaceutical Manufacturing including cGMPs, GDP, FDA, PSM, OSHA, and EPA requirements Communicates effectively in writing and verbally within the department Computer skills, in the areas of: Microsoft Office Products (Word, Excel, PowerPoint), Chemdraw, and SciFinder Ability to work interactively within a multi-functional team-oriented environment Takes initiative in setting own goals and work plans Hands-on organic chemistry laboratory experience Has a broad technical knowledge in Organic Chemistry and Process Improvement Methodology Maintains a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports Experience in the synthesis and purification of peptides (desired) Has working knowledge of all plant-scale unit operations, scale-up, and plant design considerations Understanding of chemical reactivity, potential exotherms, cross reactivity, side products, and waste streams, especially for processes they support Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneous) processes Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects Assumes reasonable risk in trying out new, self-generated ideas Proactive approach to problem identification and resolution Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective, and effective Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems or when proposing improvements Ability to provide leadership in all process chemistry aspects of manufacturing processes; leads teams in the development, transfer, troubleshooting, and improvement of chemical processes in interactive, interdisciplinary team environment Seeks out opportunities to learn manufacturing needs and methods that facilitate substantial process improvements; acquires new skills in state-of-the art technology and applies it to their assignments Demonstrates skills in negotiation and influencing others SALARY Actual pay will be based on your skills and experience BENEFITS 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service Accident Plan Critical Illness Insurance Dental Insurance Disability Insurance Employee Assistance Program Flexible Spending Account Health Insurance PPO/HSA Hospital Indemnity Plan ID Theft Protection Life Insurance Paid Parental Leave Tuition Reimbursement Wellness Program Vacation - Three Weeks 1st Year Vision Insurance EQUAL OPPORTUNITY EMPLOYER Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices. This post will expire January 16, 2026

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical, and biotech companies manufacture medicines with the ultimate goal of improving people's lives. Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being. Our People Vision We strive for excellence. We share our passion. Together, we make a difference in patients' lives. SUMMARY Acts to drive and demonstrate the technology for the planning and execution of development and implementation of chemical processes. Ensures that the chemistry is sufficient to meet goals on process yields, throughputs, and QSHE requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned: * Familiarity with general TFF/ultra filtration setup, operation, and components * Experience with lab and/or mid-large scale TFF/ultra filtration processing * Knowledge of various types of TFF filtration methods and systems * Understanding of key operating/scalable parameters for TFF/ultra filtration and ability to determine such parameters during process familiarization/optimization * Provides technical support to lab or plant processes * Works effectively in a team-oriented environment * Presents work orally and in form of written development reports * Adheres to GDP and SOPs in all aspects of work * Independently plans and executes experiments, while working in a project team, toward development of viable commercial processes * Demonstrates a clear understanding of technical issues and the requirements of a viable manufacturing process * Executes procedures, processes, and methods for solutions to chemical and technical problems on a lab or plant scale * Ensures that the chemistry is capable of meeting cost, yield, throughput, and QSHE goals on assigned processes * Leads a team to accomplish the development, transfer, or implementation of technology at a lab or plant scale * Develops and supports scalable processes and provides technical expertise and support during lab or plant operations LEADERSHIP & BUDGET RESPONSIBILITIES Demonstrates a positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons. This position has no supervisory responsibilities. Provides technical expertise to manufacturing. SAFETY & ENVIRONMENTAL RESPONSIBILITIES Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience. QUALITY RESPONSIBILITIES Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC's Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company. cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelor's Degree (BS) in Organic Chemistry and 5 years related experience and/or training; or equivalent combination of education and experience. TFF/Untra filtration experience is required; and Peptide and GMP experience is a plus. LANGUAGE SKILLS Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to develop bench scale laboratory procedures into step-by-step operating instructions for chemical operators. Ability to effectively present information to top management, public groups, and/or boards of directors. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. REASONING ABILITY Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables. Ability to apply scientific methods to experimentally prove cause and effect. CERTIFICATES, LICENSES, REGISTRATIONS Domestic and international travel required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The noise level in the work environment is usually moderate. CORE COMPETENCIES These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity. * Demonstrates a positive attitude * Strong background in chemistry or a related scientific field * Working knowledge of regulatory issues in Pharmaceutical Manufacturing including cGMPs, GDP, FDA, PSM, OSHA, and EPA requirements * Communicates effectively in writing and verbally within the department * Computer skills, in the areas of: Microsoft Office Products (Word, Excel, PowerPoint), Chemdraw, and SciFinder * Ability to work interactively within a multi-functional team-oriented environment * Takes initiative in setting own goals and work plans * Hands-on organic chemistry laboratory experience * Has a broad technical knowledge in Organic Chemistry and Process Improvement Methodology * Maintains a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports * Experience in the synthesis and purification of peptides (desired) * Has working knowledge of all plant-scale unit operations, scale-up, and plant design considerations * Understanding of chemical reactivity, potential exotherms, cross reactivity, side products, and waste streams, especially for processes they support * Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues * Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneous) processes * Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects * Assumes reasonable risk in trying out new, self-generated ideas * Proactive approach to problem identification and resolution * Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective, and effective * Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems or when proposing improvements * Ability to provide leadership in all process chemistry aspects of manufacturing processes; leads teams in the development, transfer, troubleshooting, and improvement of chemical processes in interactive, interdisciplinary team environment * Seeks out opportunities to learn manufacturing needs and methods that facilitate substantial process improvements; acquires new skills in state-of-the art technology and applies it to their assignments * Demonstrates skills in negotiation and influencing others SALARY Actual pay will be based on your skills and experience BENEFITS * 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service * Accident Plan * Critical Illness Insurance * Dental Insurance * Disability Insurance * Employee Assistance Program * Flexible Spending Account * Health Insurance PPO/HSA * Hospital Indemnity Plan * ID Theft Protection * Life Insurance * Paid Parental Leave * Tuition Reimbursement * Wellness Program * Vacation - Three Weeks 1st Year * Vision Insurance EQUAL OPPORTUNITY EMPLOYER Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices. This post will expire January 16, 2026

Would you like to join an innovative team driven by a bold vision - unleashing tools to accelerate breakthroughs in human health? Would you like to join an innovative team creating technology to power ground-breaking insights in academic, clinical, pharma and biotech research? It is an extraordinary time for Standard BioTools. Our technology is empowering customers to improve life through comprehensive health insight. We invite you to join a leading provider of indispensable life sciences tools that is accelerating global research on multiple frontiers of human health. At Standard BioTools, we are building a positive culture where our people can do the best work of their careers, informed and influenced by our core behaviors: • Keep customers front and center in all of our work • Be accountable and deliver on commitments • Drive continuous improvement • Be collaborative and work as one team: fostering communications in a learning, coaching, and helpful environment Position Summary: SomaLogic is a 200+ person privately owned biotechnology company that delivers precise and personalized health insights using its proprietary technology, which measures changes in thousands of different proteins in blood and other sample types. We are a dedicated team of science-based colleagues working to maximize health and wellness for people around the world. Come apply your laboratory skills to making healthcare better for your loved ones and the whole world. The Manufacturing Chemist will be responsible for performing a wide variety of manufacturing activities. The Technician will prepare and formulate reagents, perform routine maintenance and troubleshooting on laboratory equipment, and prepare kits for internal and external distribution. Level commensurate with experience. Key Job Responsibilities: Synthesize and purify oligonucleotides Prepare and formulate buffers and reagents according to Standard Operating Procedures. Assemble assay kits for internal and external distribution. Ensure accurate accounting of materials in the inventory management system. Perform routine maintenance and limited troubleshooting on general use laboratory equipment, such as balances, pH meters, freezers, vacuum pumps, etc. Complete all paperwork as required (batch records, cleaning logs, maintenance logs, etc.) and ensure that all required records and logs are accurately maintained. Perform work in compliance with all GMP and EH&S requirements. Ensure that work areas are maintained in a well-organized, clean and tidy manner at all times in compliance with established requirements. Qualifications: Education This position requires a Bachelors degree or an Associates degree + a minimum of 2 years of relevant experience Skills and experience Oligonucleotide synthesis experience preferred but not required Experience working in a regulated laboratory required, experience in a cGMP environment preferred GMP documentation experience, strong attention to detail Aliquoting/pipetting, buffer and mix formulation, concentration verification skills required Experienced user of Excel spreadsheets and calculations, Laboratory Information Management System (LIMS), ERP or other computerized lab/inventory database Work Environment: Work is in a typical laboratory environment with personal protective equipment use required Must be able to lift 25 lbs on a regular basis Salary Expectations: $23 - $26/ hour Range for Role: $0.00-$0.00 All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status.

Description ENVIRONMENTAL - ENVIRONMENTAL CHEMIST GSI is seeking an Environmental Chemist to support our growing environmental remediation team that is executing technical consulting work, primarily for government clients. The Environmental Chemist will be based in Boulder, Colorado but will support projects throughout the country. Remote/telework will be considered for the right candidate depending on experience (DOE). The Environmental Chemist will understand remedial process chemistry, contaminant fate and transport in environmental matrices, and field sampling and analytical laboratory methods. The Chemist will be required to have expertise in chemical data quality management of environmental analytical data. The ideal candidate will work closely with management and senior staff and work efficiently as part of the project team. The Environmental Chemist will be capable of determining appropriate analytical methodologies, screening levels, project data needs, and the scope of testing such as matrices, methods, target analytes and measurement objectives. DUTIES AND RESPONSIBILITIES Primary duties and responsibilities include (but are not limited to): Assists in preparing work plans (e.g. Uniform Federal Policy Quality Assurance Project Plans [UFP-QAPP]) and other technical reports Develops data quality objectives (DQOs), measurement performance criteria (MPCs), and measurement quality objectives (MQOs) to meet the project-specific performance standards Determines appropriateness of sampling and analytical methods and laboratory quality systems Coordinates with the laboratory and data validator during contract execution Verifies laboratory qualifications, makes recommendations for laboratory selection, and prepares requests for quotes from laboratories Prepares data validation reports or reviews subcontractor data validation reports Conducts or oversees all on-site analytical testing including field-screening tests; including training personnel on sample collection, labeling, packaging, and shipping techniques and preparation of labels/chains of custody. Collects, evaluates, compiles, and analyzes project-specific data Performs data review and ensures accuracy and quality of internal and external work products per contract, regulatory, and work plan specifications Manages analytical laboratory data, including tabulation of results and submission into various databases (e.g. EPA SEDD) Oversees chemistry related QA/QC activities Notifies the management team of any chemistry related problems or nonconformance issues and monitors corrective action, as required Supports the preparation of proposals for Chemistry related tasks Participates in client meetings Addresses technical comments from clients, customers, and regulators MINIMUM QUALIFICATIONS, SKILLS, AND EDUCATIONAL REQUIREMENTS Minimum 5 years of directly related environmental chemistry experience Bachelor of Science degree in chemistry, engineering, environmental, biological, physical sciences or similar related field An advanced degree in one of the above disciplines may be substituted for equivalent experience Knowledge of environmental analytical chemistry methodologies, chemistry of remedial treatment technology, chemical fate and transport, and experience in the sampling and analysis of toxic/hazardous chemicals in environmental matrices. Familiarity with the Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) and the Resource Conservation and Recovery Act (RCRA) Familiarity with DoD QSM and DoD ELAP Good working knowledge of word-processing and integrated software applications including MS Office and MS Excel Ability to work on multiple projects of various size and scope Ability to work independently and as a member of a project team Good communication and documentation skills Ability to pass a background check (as required for project work) DESIRABLE SKILLS AND EXPERIENCE Experience with Department of Defense projects and supporting the USACE, US Army, USAF, and/or NAVFAC clients and customers Experience with the National Environmental Policy Act Experience with federal analytical databases, such as FUDSChem, ERPIMS, HQAES, and NIRIS. Experience with emerging contaminants (e.g. PFAS compounds) Familiarity with the Military Munitions Response Program (MMRP) TRAVEL REQUIREMENTS Minimal travel is required and expected about 0-5% of the year; overnight travel is required. Travel is anticipated to consist primarily of client visits, conferences, and work at partner offices across the United States. We are committed to a merit-based hiring process that values individual skills, qualifications, and performance. Our hiring practices comply with all applicable federal, state, and executive orders, including the recent Executive Order on Equal Opportunity Hiring.

RESEARCH CHEMIST/CHEMICAL ENGINEER Rocky Mountain Scientific Laboratory Department:Advanced Chemistry & Chemical Processing Group Yes Travel:No Schedule:Full-time Description of Business Environment: Peace is often associated with passivity. At Rocky Mountain Scientific Laboratory, we associate peace with strength, courage, and action. We know that enabling peace to prevail is not for the faint of heart, which is why we built our company foundation on the core values of Integrity, Quality, Agility, and Grit. We pride ourselves in providing unequaled services and technologies in the field of applied energetics to our customers. Our experts possess extensive knowledge and capability in energetic materials and military systems enabling them to offer analytical characterization, modeling & simulation, design, system integration, prototyping, test engineering, and proof-of-concept production services covering a wide range of applications. Our strengths lie in our ability and relentless determination to get the job done quickly and affordably. RMSL is an Equal Employment Opportunity (EEO), Affirmative Action employer and welcomes all qualified applicants. All qualified applicants will receive fair and impartial consideration for employment without regard to race, color, religion, sex, age, disability, veteran status, national origin or other legally protected status. An applicant with a disability or a disabled veteran can request reasonable accommodation to apply for one of our positions. Specific Job Description: RMSL is a growth company with an outstanding job opportunity for a Research Chemist. This position will report to the Advanced Chemistry & Chemical Processing Group Lead. The Research Chemist/Chemical Engineer will be an integral part of a small cross functional team working on exciting development projects with cutting-edge technology. In this role, the ideal candidate will have a strong background in Chemistry/Chemical Engineering with experience in organic and/or inorganic synthesis. This role will be a part of an integrated team focused on the development of novel energetic systems, energetic material scale-up processes, development of ammunition and armaments, testing and analysis of energetic materials. This individual must demonstrate innovation, an ability to learn, out-of-the-box thinking and creativity. Duties Include: Develop novel synthesis and scale-up processes Characterize novel energetic materials using a variety of analytical methods Formulation optimization of propellants, pyrotechnics, and explosive formulations Handling and testing of energetic materials, armaments, and weapon systems Integrate energetic materials in to end articles such as ammunition and munitions. Ability to handle materials with strict adherence to safety process requirements Design of experiments and test series that result in safe and efficient collection of data Design, source selection, installation, maintenance, and operation of specialized instrumentation and testing equipment Assistance with company compliance in restricted information security regulations Project engineering tasks such as report writing, technical presentations (at customer and public meetings), and technical deliverables tracking Required Skills: Problem solver that can work in a team environment on fast pace projects Hands-on experience with energetic materials Proficient in standard laboratory practices Exercises creative thinking and innovation Strong verbal and written communication skills Physical requirements: Must be able to sit for extended periods of time; must be able to lift up to 50 lbs.; must have the ability to see near and far and work with a computer monitor Required to bend, sit, stand and lift to perform job effectively Highly Beneficial Skills: Familiar with general explosive effects and chemistry Experience in one or more of the following areas Continuous Synthesis Armament and munition development Energetic material synthesis and formulation Laboratory and pilot plant scale-up of energetic materials Knowledge of basic-intermediate chemistry and/or chemical engineering Experience with chemical formulation development Minimum Qualifications: Must have a BS or higher in Chemistry or Chemical Engineering Ability to obtain security clearance Ability to obtain CO State Blasters Permit Benefits: Medical insurance Dental insurance Vision insurance 401(k) with matching Disability insurance Life insurance Paid time off Professional development Flexible schedule

The National Food Lab is a fast-growing company with a vision to be the destination for tailored solutions for the food industry - beginning to end. Our mission is to provide services that help food, beverage, and supplement companies deliver safe, healthy and successful products. We seek to make a positive impact in the advancement of food safety, quality and nutrition, fulfilling our corporate promise - to improve health and improve lives. The National Food Lab's best-in-class consumer and sensory research capabilities employ a variety of quantitative and qualitative consumer and sensory research techniques to help our clients make products consumers love. We help our clients: Develop new product ideas Re-energize a well-established product Assess product-concept fit or packaging effectiveness Understand the product, brand and category competitive landscapes Present objective results to management Job Description A Food Scientist is well versed in all phases of the food product development cycle and can work independently to develop a new product from conception through plant scale-up. May supervise the work of junior professionals such as Technicians, Interns and On-Call staff. Essential Duties and Responsibilities Demonstrates and promotes the company vision. Regular attendance and punctuality Applies GMP/GLP in all areas of responsibility, as appropriate. Plans and designs specific activities required by the projects and distributes activities to Laboratory Technologist or Intern based on skill sets. Executes experimental, analytical, and sensory work on both bench and pilot scale. Develops analytical methods and coordinates nutritional and component analysis. Writes reports, formulas, data and communication that is thorough and ready for the client with little or no editing required by supervisor. Ensures all samples are prepared with good GMP's that are well labeled and of high quality. Ensures lab notebook maintenance SOP is followed. Seeks out information/facilities to get the job completed. Collaborates with internal and external resources (suppliers, consultants, professors, service providers and other third-party people) to find solutions. Ensures appropriate and timely communication of key information among client, team, and supervisor. Establishes and maintains professional rapport with client. Adds insight and value to discussions, understanding client needs. Organizes and participates in meetings and conference calls. Reads and responds to emails, phone calls in a timely manner. Assists team members to carry out such communication duties as necessary. Independently coordinates pilot and plant trials develops trial plans and protocols, serves as liaison between the manufacturing plant, client, and development laboratory for trial. Independently drafts, structures, and executes project plans. Submits to supervisor for review. Identifies appropriate phases and deliverables and determines resource needs. Writes pilot and plant trial reports. Maintains documentation; Organizes computer and hard copy files and records in lab notebook for corporate records and sharing. Keeps updated and educated on relevant news, literature, and findings in the industry. Trains less-experienced staff Performs other related duties as assigned. Travels to various NFL and client locations to support studies and projects. Travels to technical conferences to represent TheNFL. Conducts all activities in a safe and efficient manner. Performs other duties as assigned. Will be exposed to potential food allergens. Required to handle and evaluate all types of foods and ingredients derived from plants, animals and synthetically manufactured. Qualifications To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required. Education Minimum Required: PhD degree from an IFT accredited food science program, or equivalent combination of education and experience Experience Minimum Required: Non-PhD candidates would have a minimum of 2 years practical experience in product or process development Additional Information A salaried range for this position is between $70,000-$75,000 Other Factors: Overtime and weekend work as plants required Will be exposed to potential food allergens Must use hearing protection, eye protection, proper footwear, lab coat, hairnets and gloves when necessary. Travel Requirements: Occasionally (up to approximately 10% of time) has to travel overnight, weekends, interstate or international where air travel is required. Travel is primarily to: Client facilities, manufacturing facilities and other NFL/Eurofins sites What Happens Next: Our people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths. What we Offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

The National Food Lab is a fast-growing company with a vision to be the destination for tailored solutions for the food industry - beginning to end. Our mission is to provide services that help food, beverage, and supplement companies deliver safe, healthy and successful products. We seek to make a positive impact in the advancement of food safety, quality and nutrition, fulfilling our corporate promise - to improve health and improve lives. The National Food Lab's best-in-class consumer and sensory research capabilities employ a variety of quantitative and qualitative consumer and sensory research techniques to help our clients make products consumers love. We help our clients: Develop new product ideas Re-energize a well-established product Assess product-concept fit or packaging effectiveness Understand the product, brand and category competitive landscapes Present objective results to management Job Description A Food Scientist is well versed in all phases of the food product development cycle and can work independently to develop a new product from conception through plant scale-up. May supervise the work of junior professionals such as Technicians, Interns and On-Call staff. Essential Duties and Responsibilities Demonstrates and promotes the company vision. Regular attendance and punctuality Applies GMP/GLP in all areas of responsibility, as appropriate. Plans and designs specific activities required by the projects and distributes activities to Laboratory Technologist or Intern based on skill sets. Executes experimental, analytical, and sensory work on both bench and pilot scale. Develops analytical methods and coordinates nutritional and component analysis. Writes reports, formulas, data and communication that is thorough and ready for the client with little or no editing required by supervisor. Ensures all samples are prepared with good GMP's that are well labeled and of high quality. Ensures lab notebook maintenance SOP is followed. Seeks out information/facilities to get the job completed. Collaborates with internal and external resources (suppliers, consultants, professors, service providers and other third-party people) to find solutions. Ensures appropriate and timely communication of key information among client, team, and supervisor. Establishes and maintains professional rapport with client. Adds insight and value to discussions, understanding client needs. Organizes and participates in meetings and conference calls. Reads and responds to emails, phone calls in a timely manner. Assists team members to carry out such communication duties as necessary. Independently coordinates pilot and plant trials develops trial plans and protocols, serves as liaison between the manufacturing plant, client, and development laboratory for trial. Independently drafts, structures, and executes project plans. Submits to supervisor for review. Identifies appropriate phases and deliverables and determines resource needs. Writes pilot and plant trial reports. Maintains documentation; Organizes computer and hard copy files and records in lab notebook for corporate records and sharing. Keeps updated and educated on relevant news, literature, and findings in the industry. Trains less-experienced staff Performs other related duties as assigned. Travels to various NFL and client locations to support studies and projects. Travels to technical conferences to represent TheNFL. Conducts all activities in a safe and efficient manner. Performs other duties as assigned. Will be exposed to potential food allergens. Required to handle and evaluate all types of foods and ingredients derived from plants, animals and synthetically manufactured. Qualifications To perform this job successfully , the individual must be able to perform each essential duty satisfactorily. The requirements below are representative of the knowledge, skill or ability required. Education Minimum Required: PhD degree from an IFT accredited food science program, or equivalent combination of education and experience Experience Minimum Required: Non-PhD candidates would have a minimum of 2 years practical experience in product or process development Additional Information A salaried range for this position is between $70,000-$75,000 Other Factors: Overtime and weekend work as plants required Will be exposed to potential food allergens Must use hearing protection, eye protection, proper footwear, lab coat, hairnets and gloves when necessary. Travel Requirements: Occasionally (up to approximately 10% of time) has to travel overnight, weekends, interstate or international where air travel is required. Travel is primarily to: Client facilities, manufacturing facilities and other NFL/Eurofins sites What Happens Next: Our people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths. What we Offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

At Weston Solutions, Inc. you will do meaningful work and make valuable contributions. Employee ownership at Weston is a path to professional growth and access to diverse opportunities in a highly connected community that works together across key service areas to make a difference in the environment. Weston has continued to evolve and adapt to our changing world as a premier provider of environmental and infrastructure services for over sixty years. In both the public and private sectors our teams help identify, solve, mitigate, and manage critical environmental issues to help clients achieve a more sustainable future. Weston Solutions is seeking a Associate Scientist (Chemist) to support environmental consulting work for our Federal, State, Local and Commercial/Industrial clients. This candidate will provide our clients with accurate and pertinent scientific data according to the methods, procedures, and techniques. The candidate will support field work and operate mobile field analytical instruments, assist with method development, calibrate and maintain field equipment. The position may also be on-call periodically to support emergency response projects as needed. Location: Lakewood, CO Knowledge, Skills & Abilities: * BS or equivalent in Chemistry and 2-4 years of experience in the environmental field and/or an analytical laboratory environment. * Experience in analytical method selection, data management, and interpretation. * Exposure to various technical and scientific analytical procedures. * Ability to work independently and as part of a team, be highly adaptable, flexible, and amenable to working in non-standard environments. * Strong interpersonal communication, organizational, analytical, and technical writing skills. * Ability to conduct fieldwork throughout the U.S. and carry up to 50 lbs. of field gear in challenging conditions including extreme weather conditions. * Valid driver's license and ability to work on-call and mobilize into the field with little or no notice. * Proficient in Microsoft Office and Adobe Acrobat. Preferred Skills: * Experience in maintaining and calibrating laboratory instrumentation, such as GC & GC/MS * Experience with EPA and other analytical methods, best laboratory practices, and QA/QC procedures * Field instrumentation. Proficient in the use of various air and water monitoring instruments (PID/FID, multi gas meters, etc.). Abilities include calibration of field instruments, implementation in field, and interpretation of results. * Experience writing technical documents such as Standard Operating Guidance and Procedures * Experience with soil, water, air or multi-media sampling strategies and protocols * Current OSHA 40-HR HAZWOPER certification desirable but not required Technical and Operational Scope: * Develop field operating procedures and technical documentation related to oil spills, hazardous substance releases, biological agents, chemical warfare agents, radiation, and/or weapons of mass destruction * Participate in field work as a member of sampling teams * Analyze and interpret analytical data and perform laboratory data review and validation * Author, review and revise technical documents and plans including analytical methods, Standard Operating Guidance, and Standard Operating Procedures * Calibration and maintenance of a variety of multi-media monitoring and sampling equipment. * Exercises judgment on applicability of methods and approaches in use and determines best approaches to problem solving when standard procedures are inadequate. * Determines best method of data gathering, database management, and analysis of data to achieve project goals. * Consults with outside specialists to obtain most accurate and timely data possible while meeting project specifications and timetables. * Occasional travel and outdoor field work at hazardous waste sites. * Document field activities and prepare daily and final reports for clients within established budgets and schedules. We fully invest in our people: Weston provides a generous, comprehensive benefits package program that offers employees high value options with solid financial protection, meeting the personal needs of its people and their families. * Medical, Dental, Vision, 401K with base and matching employer stock contributions. * Paid time off includes personal, holiday and parental. * Life and disability plans. * Critical illness and accident plans. * Work/Life flexibility. * Professional development opportunities. Compensation will vary based upon experience, education, skill level, and other compensable factors.

Full-time Description At SPL, we turn science into impact. We're searching for a driven Laboratory Analyst to join our team in Commerce City, CO. In this role, you'll be trained by industry experts, work with advanced laboratory technology, and deliver the accurate data our clients rely on for compliance and decision-making. Every analysis you perform helps ensure cleaner water, safer communities, and a healthier world. If you're ready to build technical expertise, expand your analytical skills, and grow your career in a collaborative, purpose-driven lab, we want to hear from you! Why You'll Love This Role Perform on the front line of environmental analysis by generating analytical data to support environmental compliance and decision-making; Grow hands-on skills in analytical instrumentation, Laboratory Information Management Systems (LIMS), and advanced testing methods; Gain exposure to real-world applications in environmental science, regulatory compliance, and client services; Join a team where your contributions directly support public safety, regulatory standards, and cleaner environments. What You'll Do Perform sample preparation and analytical testing in accordance with approved methods and established protocols to ensure accuracy, timeliness, and regulatory compliance; Enter and manage data in the Laboratory Information Management System (LIMS) or other designated systems; Develop and maintain proficiency with a broad range of analytical equipment, laboratory software platforms, and technology relative to assigned analyses; Review and interpret results to ensure accuracy and completeness; Document all work clearly, maintaining traceable laboratory records; Perform routine equipment checks, troubleshooting, calibrations, and preventative maintenance; Adhere to quality systems, SOPs, and continuous improvement initiatives; Follow and promote Good Laboratory Practices (GLP) and all health, safety, and environmental standards; Assist with general laboratory housekeeping, glassware cleaning, inventory, and supply management; Participate in cross-training to support workload balance and operational needs; Perform other duties as assigned. Requirements What Makes You a Great Fit Bachelor's Degree in Science or related field; Previous hands-on experience in a professional or academic lab setting; Ability to manage and process high volumes of samples efficiently; Proficiency with Microsoft Office tools (Word, Excel, Outlook) and Adobe Acrobat. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 9 paid holidays plus a generous PTO plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position following a Monday through Friday schedule with daily shift hours from 7:30 am - 6 pm; Must be able to work outside of normal hours to support business needs and deadlines; Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future. Salary Description $22-$26 per hour

Job Description This position functions primarily in a classified ISO-8 environment and requires the individual to wear appropriate PPE. This position will perform dispensing and formulation operations and perform other duties, such as cleaning, restocking, visual inspection, and labeling, as required and/or assigned. All assigned tasks must be conducted in adherence with all applicable procedures, cGMPs, company policies and any other quality or regulatory (Ex: OSHA, DEA, FDA, etc.) requirements. Facility is a multiple shift operation where variable shifts, including weekends, may be required. Schedule: Tuesday to Friday 3 PM Until 1:30 AM (or until work is completed) Pay: $25/hour SAFETY Strictly adhere to all cGMP, health and safety requirements, procedures, and corporate policies. Authorized to immediately stop any task that is determined to be an imminent hazard. Always promote and demonstrate safe work practices and adhere to PPE requirements. Safely handle chemicals, corrosives, solvents, and other pharmaceutical compounds. Demonstrate physical ability to lift a minimum of 50 lbs. and push/pull pallets, product cans, etc. multiple times per shift. PRIMARY RESPONSIBILITIES: Perform ISO-8 dispensing and formulation operations consistent with established protocols, procedures, and regulatory/cGMP requirements. Learn to utilize all relevant equipment/technology for formulation operations. Complete and document required training to gain proficiency for all assigned job tasks. Accurately and contemporaneously document all actions performed per GDP standards. Assist with classified and non-classified area cleaning and maintenance as required. Perform visual inspection, labeling, and additional support tasks as required. Make recommendations for process improvements. Possess the ability to master multiple processes across different areas. Recognize and respond appropriately to equipment/documentation issues and deviations; obtain appropriate clarification and guidance from leadership before proceeding. Maintain a quality focused, “Right First Time”, attitude. Arrive for work on-time, prepared to work in the classified environment for the majority of each shift. Operate with Integrity by maintaining high ethical standards. Treat all employees with trust, respect, and professionalism. Speak up and hold others accountable for high integrity by providing constructive feedback. Take accountability for individual and team mistakes and participate in related corrective actions. Ensure patient safety by understanding you and your team's impact on product quality. Excel within a diverse and high performing team. Remain open to new ideas and perspectives, communicate across shifts as required, and comply with site process to create a safe work environment. Demonstrate a passion to perform by meeting personal and departmental goals. Self-driven and self-accountable, performs required tasks, and progresses on qualifications within reasonable timelines. Demonstrate innovation abilities by identifying and speaking up about viable options for improvements and exploring and creating a path for implementation. High School Diploma or equivalent. Must pass a drug test. Must speak, write, and read English. Must be a team player. Must have excellent attention to detail. Prior Sterile Compounding and Pharmaceutical Industry experience. Prior experience operating manufacturing equipment/machinery. Knowledge of FDA guidelines, cGMP, and GDP. Willingness to participate in training and gain other certifications as needed. Knowledge of basic arithmetic and chemistry calculations. Ability to work in a fast-paced environment with dynamic priorities and demands. Excellent written and verbal communication skills. Desire to expand knowledge and grow with the company. Leadership ability.

ABOUT YOU Are you passionate and ready to join an inclusive work environment, committed to leading new ideas and pathways, and to delivering value? If the answer is, “Yes!” then we have an exciting career opportunity for you as a Laboratory Technician based in our Denver, CO laboratory. Who are we? We are Enthalpy Analytical, a subsidiary of Montrose, a global environmental services provider offering environmental planning and permitting, measurement and analytical services, and environmental resiliency and sustainability solutions. Our qualified engineers, scientists, technicians, associates, and policy experts are proud of our collective expertise and the collaborative nature of our approach to helping clients. We strive to optimize environmental resiliency in a way that effectively complements our clients' decision-making and operations and efficiently fulfills their project requirements. We have 135 offices across the United States, Canada, Europe and Australia and over 3,000 employees - all ready to provide solutions for environmental needs. WHAT WE CAN OFFER YOU As a key member of our Montrose team, you can expect: Mentorship and professional development resources to advance your career Direct exposure to our industry's leading experts who are solving the world's toughest environmental challenges An entrepreneurial environment where you can learn, thrive and collaborate with talented colleagues Opportunities to engage and contribute in our Diversity, Fairness and Inclusion and Women Empowering Leadership employee resource groups Competitive compensation package: Starting hourly wages ranging from $23.00 - $25.00, commensurate with accomplishments, performance, credentials and geography Competitive medical, dental, and vision insurance coverage 401k with a competitive 4% employer match Progressive vacation policies, company holidays and paid parental leave benefits to ensure work/life balance A financial assistance program that supports peers in need, known as the Montrose Foundation Access to a student loan planning tool to optimize your student loan payoff plans and compare student loan rates with lenders. A DAY IN THE LIFE Enthalpy Analytical, is part of the larger organization, Montrose Environmental Group, is comprised of 9 laboratories servicing air, water, and soil testing. Regulations drive the need for our services, but our unique capabilities allow us to add value to clients beyond environmental compliance. Our Denver, CO laboratory is currently seeking a Full-Time Laboratory Technician to join our Metals Department. Compensation: $23.00-$25.00 Schedule: Tuesday - Saturday or Sunday - Thursday , 2:00pm - 10:00pm As a key member of the laboratory team, this role will be responsible for a full range of activities including: Capable of high-throughput preparation of environmental samples for metals testing. Proficiency using analytical equipment including: balances, pipettes, bottle top dispensers, hot blocks, and volumetric/graduated glassware. Daily monitoring of sample scheduling to ensure that samples are processed within EPA's and methods' holding time Schedule workload in order to process samples within clients expected due dates Routine sample preparation according to Standard Methods and EPA methods Performs analyst's review of data and QC Reviews of QA/QC criteria for batch acceptance Adheres to Standard Operating Procedures and follow safe work practices Participates in instruments' preventative maintenance and trouble shooting Participates in focus teams to improve efficiency Be flexible in work schedule including overtime when needed React to change productively and handle other essential tasks as assigned Performing other duties and responsibilities as prescribed by the Company Compliance with Enthalpy's Quality Assurance Program and other policies YOUR EXPERTISE AND SKILLS To perform this job successfully, individuals must be able to perform each duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. High School Diploma Bachelor's degree in any science field is a plus Minimum 1 year of lab experience preferred Knowledge of general lab practices and lab safety Knowledge of basic laboratory techniques preferred (knowledge of PPE, use of balance, pipetting, glassware handling, etc.) Experience in metal preparation is a plus Ability to lift and carry a minimum of 25 lbs. Ability to remain in a stationary position for extensive periods of time Preferred Skills Knowledge of analytical method, analytical instruments, general lab practices and lab safety Must be flexible in work schedule and able to work overtime Good organizational and communication skills Ability to multi-task Ability to work independently and make sound decisions The above statements are intended to describe the general nature of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties and skills required of employees so classified. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact ************ or ************************ for assistance. MAKE THE MOVE TO ACCELERATE YOUR CAREER We are a fast-paced, dynamic and high-growth company. You are your own boss, but you will get tons of guidance and plenty of support from talented, super-smart colleagues and its service providers. Therefore, if freedom, autonomy, and head-scratching professional challenges attract you, we could be the perfect match made in heaven. Want to know more about us? Visit montrose-env.com and have fun! Montrose is an Equal Opportunity Employer. Montrose is committed to recruiting and hiring qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status. Montrose is committed to providing access and reasonable accommodation in its employment for individuals with disabilities.

Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: * Accurately perform and read test results and notify Laboratory Management of deviations * Prepare and analyze samples for indicator organisms, pathogens, and chemistries * Apply aseptic/microbiological techniques in daily workload * Report inventory and expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control * Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements * Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends * Perform all activities in a neat, safe, hygienic, and efficient manner * Share information in an open and timely manner * Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team * Responsible for the safety of oneself and others working within their area Supervision: * This job does has no supervisory responsibilities. Education & Experience: * Associate degree in Life Science or related field with two or more years of laboratory experience, preferred * Two or more years of experience in a commercial food-testing or analytical laboratory * Or equivalent combination of education and experience * Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures * Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures * Broad knowledge of concepts, practices, and procedures of a food testing laboratory * Ability to travel when necessary Physical Demands/Work Environment: * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks * Overnight Travel is required at the discretion of management * Occasionally lift and/or move up to 25 pounds * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Tuesday - Saturday 9pm-5:30am

Department: Quality Employment Type: Full-Time Compensation: $75,00-$100,000 VPI is a leader in high-quality, specialized pharmaceutical compounding, dedicated to patient safety and therapeutic efficacy. We empower healthcare professionals with innovative, customized medications that meet unique patient needs. This role is essential to our mission, ensuring every product released meets the highest standards of quality and compliance. VPI Compounding is seeking a highly skilled and meticulous Analytical Chemist to join our dedicated Quality team. This critical role is responsible for the integrity, safety, and efficacy of our compounded pharmaceutical products. The successful candidate will perform chemical analyses, lead method development, and drive compliance with rigorous regulatory standards, serving as a pillar of our commitment to quality. Key Responsibilities: Chemical Analysis & Quality Assurance Execute complex qualitative and quantitative analysis of raw materials, in-process samples, and finished pharmaceutical products. Expertly operate, troubleshoot, and maintain advanced analytical instrumentation, including High-Performance Liquid Chromatography (HPLC), Mass Spectrometry (MS), and UV/Vis spectrophotometry. Method Development & Validation Design, develop, and rigorously validate new analytical testing methods for novel and existing pharmaceutical compounds. Strategically optimize existing testing procedures to significantly enhance laboratory throughput, accuracy, and efficiency. Regulatory Compliance & Documentation Implement and strictly uphold quality control procedures in full compliance with FDA regulations, cGMP guidelines, and all internal Standard Operating Procedures (SOPs). Prepare comprehensive, detailed reports and documentation packages necessary to support regulatory submissions and internal quality audits. Collaboration & Innovation Serve as the key analytical partner to the Formulation Team, providing data-driven insights to support product consistency and innovation. Maintain a current understanding of advancements in analytical techniques and pharmaceutical compounding to continuously elevate laboratory practices. Qualifications: Education & Experience: : Bachelor's degree in Chemistry, Analytical Chemistry, or a closely related scientific field. (Master's or PhD highly preferred) Minimum of 2 years of hands-on experience in an analytical chemistry laboratory, preferably within a pharmaceutical, regulated, or compounding environment. Proven technical expertise operating and maintaining advanced chromatographic and spectroscopic equipment. Skills & Attributes: Exceptional attention to detail and ability to execute complex procedures accurately. Strong verbal and written communication skills to effectively report technical data and findings. Demonstrated problem-solving abilities in a laboratory setting. Physical Requirements: Ability to perform fine motor movements necessary for laboratory work. Must be able to work at a computer workstation for extended periods. Benefits: Company-paid health, dental, and vision insurance (Premiums covered by VPI) 401(k) with employer match Paid Holidays, Floating Holidays, and PTO Tuition and Certification Reimbursement RTD EcoPass for public transportation Opportunities for professional growth and development Equal Opportunity Employer: VPI Compounding Pharmacy is an Equal Employment Opportunity (EEO) employer. We are committed to providing equal opportunity for all qualified persons employed by or seeking employment with VPI, regardless of race, color, creed, religion, sex, sexual preference, national origin, age, marital status, veteran status, or non-job related handicaps. This policy extends to all areas of employment, including recruitment, job assignment, promotion, and other terms of employment.

RESEARCH CHEMIST TECHNICIAN Rocky Mountain Scientific Laboratory Department:Advanced Chemistry & Chemical Processing Group Yes Travel:Yes Schedule:Full-time Description of Business Environment: Peace is often associated with passivity. At Rocky Mountain Scientific Laboratory, we associate peace with strength, courage, and action. We know that enabling peace to prevail is not for the faint of heart, which is why we built our company foundation on the core values of Integrity, Gratitude, Mission Driven, and Grit. We pride ourselves in providing unequaled services and technologies in the field of applied energetics to our customers. Our experts possess extensive knowledge and capability in energetic materials and military systems enabling them to offer analytical characterization, modeling & simulation, design, system integration, prototyping, test engineering, and proof-of-concept production services covering a wide range of applications. Our strengths lie in our ability and relentless determination to get the job done quickly and affordably. RMSL is an Equal Employment Opportunity (EEO), Affirmative Action employer and welcomes all qualified applicants. All qualified applicants will receive fair and impartial consideration for employment without regard to race, color, religion, sex, age, disability, veteran status, national origin or other legally protected status. An applicant with a disability or a disabled veteran can request reasonable accommodation to apply for one of our positions. Specific Job Description: RMSL is a growth company with an outstanding job opportunity for a Research Chemist Technician. This position will report to the Advanced Chemistry & Chemical Processing Group Manager. The Research Chemist Technician will be an integral part of a small cross functional team working on exciting development projects with cutting-edge technology. In this role, the ideal candidate will have a strong background in Chemistry with experience in organic and/or inorganic synthesis. This role will be a part of an integrated team focused on the development of novel energetic systems, energetic material scale-up processes, development of ammunition and armaments, testing and analysis of energetic materials. This individual must demonstrate innovation, an understanding of the fundamentals of engineering, an ability to learn, out-of-the-box thinking and creativity. Duties Include: Assist in the synthesize energetic materials and scale-up process Characterize novel energetic materials using a variety of analytical methods (DSC, TGA, SDT, TAM, Particle Size Analyzer, GC-FID, ARSST, UV-VIS-NIR, FTIR and Raman spectroscopy) and material sensitivity characterization (BAM friction, impact, and ESD testing) Ability to handle hazardous materials with strict adherence to safety process requirements Assist in the design of experiments and test series that result in safe and efficient collection of data Installation, maintenance, and operation of specialized instrumentation and testing equipment Project engineering tasks such as report writing, technical presentations (at customer and public meetings), and technical deliverables tracking Required Skills: Problem solver that can work in a fast-paced team environment on projects Hands-on experience with energetic materials Proficient in standard laboratory practices Exercises creative thinking and innovation Strong verbal and written communication skills Physical requirements: Must be able to sit for extended periods of time; must be able to lift up to 50 lbs.; must have the ability to see near and far and work with a computer monitor on a daily basis Required to bend, sit, stand and lift to perform job effectively Highly Beneficial Skills: Familiar with general explosive effects and chemistry Experience in one or more of the following areas Additive manufacturing (AM) Energetic material or hazardous material synthesis Laboratory and pilot plant scale-up of energetic or hazardous materials LabRAM operation Knowledge of basic-intermediate chemistry and/or chemical engineering Minimum Qualifications: Must have an AS, BS and/or MS in Chemical Engineering or Chemistry Ability to obtain security clearance Ability to obtain CO State Blasters Permit Benefits: Medical insurance Dental insurance Vision insurance 401(k) with matching Disability insurance Life insurance Paid time off Professional development Flexible schedule

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical, and biotech companies manufacture medicines with the ultimate goal of improving people's lives. Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being. Our People Vision We strive for excellence. We share our passion. Together, we make a difference in patients' lives. SUMMARY Performs analytical research and development activities for the purpose of designing/improving a manufacturing process or technology by performing the following duties. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned. * Participates in development of new processes by applying analytical skills and training * Participates in the development of new and innovative analytical chemistry and methodology, supporting manufacturing, and regulatory needs. Facilitates and supports analytical technology transfers * Participates in the development of key technologies and transfer strategies that function well in a manufacturing environment * Plans and formulates aspects of analytical research and development proposals such as objectives or purpose of project, applications that can be utilized from findings, cost of project, equipment, and human resource requirements * Develops, implements, and validates analytical methods and procedures * Keeps accurate records and documents experimentation * Develops a comprehensive understanding of internal, corporate, and ICH stability guidelines to provide support to the Corden Pharma Stability Program * Participates in manufacturing site activities, such as troubleshooting and analytical problem resolving * Develops an understanding of QEH&S principles and regulatory affairs * Analyzes batches of drug substance, intermediates and raw materials to be used in clinical or registration programs * Responsible for properly managing the generation and accumulation of hazardous and non-hazardous waste * Works flexible hours including weekends and nights to accommodate the production/validation schedule LEADERSHIP & BUDGET RESPONSIBILITIES Demonstrates positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons. SAFETY & ENVIRONMENTAL RESPONSIBILITIES Every individual is personally responsible for the safety and environmental aspects of his or her activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability and experience. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE Bachelor's degree in Chemistry or related sciences with 3 years of relevant experience. LANGUAGE SKILLS Ability to read, analyze, and interpret common scientific and analytical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to write speeches and articles for publications that conform to prescribed style and format. Ability to effectively present information to top management, public groups, and/or boards of directors. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply statistical concepts such as significant figures and analysis of variance. REASONING ABILITY Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. CERTIFICATES, LICENSES, REGISTRATIONS Domestic and international travel required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to work with hands; and talk or hear. The employee frequently is required to stand, walk, and sit. The employee is occasionally required to reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee frequently uses toxic and/or caustic chemicals as well as high potent compounds and there is a risk of exposure. The employee is occasionally exposed to moving mechanical parts, outside weather conditions, and risk of electrical shock. The noise level in the work environment is usually moderate. CORE COMPETENCIES These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity. * Presentation and persuasion skills * Developed written and verbal communication skills SALARY Actual pay will be based on your skills and experience. BENEFITS * 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service * Accident Plan * Critical Illness Insurance * Dental Insurance * Disability Insurance * Employee Assistance Program * Flexible Spending Account * Health Insurance PPO/HSA * Hospital Indemnity Plan * ID Theft Protection * Life Insurance * Paid Maternity/Paternity Leave * Tuition Reimbursement * Wellness Program * Vacation - Three Weeks 1st Year * Vision Insurance EQUAL OPPORTUNITY EMPLOYER Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices. This posting will expire on Dec 22, 2025 but may be extended.

Full-time Description At SPL, we turn science into impact. We're searching for a driven Laboratory Analyst to join our team in Greeley, CO. In this role, you'll be trained by industry experts, work with advanced laboratory technology, and deliver the accurate data our clients rely on for compliance and decision-making. Every analysis you perform helps ensure cleaner water, safer communities, and a healthier world. If you're ready to build technical expertise, expand your analytical skills, and grow your career in a collaborative, purpose-driven lab, we want to hear from you! Why You'll Love This Role Perform on the front line of environmental analysis by generating analytical data to support environmental compliance and decision-making; Grow hands-on skills in analytical instrumentation, Laboratory Information Management Systems (LIMS), and advanced testing methods; Gain exposure to real-world applications in environmental science, regulatory compliance, and client services; Join a team where your contributions directly support public safety, regulatory standards, and cleaner environments. What You'll Do Perform sample preparation and analytical testing in accordance with approved methods and established protocols to ensure accuracy, timeliness, and regulatory compliance; Enter and manage data in the Laboratory Information Management System (LIMS) or other designated systems; Develop and maintain proficiency with a broad range of analytical equipment, laboratory software platforms, and technology relative to assigned analyses; Review and interpret results to ensure accuracy and completeness; Document all work clearly, maintaining traceable laboratory records; Perform routine equipment checks, troubleshooting, calibrations, and preventative maintenance; Adhere to quality systems, SOPs, and continuous improvement initiatives; Follow and promote Good Laboratory Practices (GLP) and all health, safety, and environmental standards; Assist with general laboratory housekeeping, glassware cleaning, inventory, and supply management; Participate in cross-training to support workload balance and operational needs; Perform other duties as assigned. Requirements What Makes You a Great Fit Associate's or Bachelor's Degree in Science or related area strongly preferred; Equivalent experience may be considered in lieu of degree; Previous hands-on experience in a professional or academic lab setting strongly preferred; Ability to manage and process high volumes of samples efficiently; Hard working, tenacious, and committed to delivering high-quality, defensible data; Strong problem identification and problem-solving skills; Strong accountability, attention to detail, and ability to work independently and as part of a team; Proficiency with Microsoft Office tools (Word, Excel, Outlook) and Adobe Acrobat. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 9 paid holidays plus a generous PTO plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position following a standard Monday through Friday schedule; Flexibility to work outside of normal hours to support business needs and deadlines; Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future. Salary Description $20-$24 per hour

Job Description Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: Accurately perform and read test results and notify Laboratory Management of deviations Prepare and analyze samples for indicator organisms, pathogens, and chemistries Apply aseptic/microbiological techniques in daily workload Report inventory and expendable supplies/materials needed for testing requirements Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends Perform all activities in a neat, safe, hygienic, and efficient manner Share information in an open and timely manner Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team Responsible for the safety of oneself and others working within their area Supervision: This job does has no supervisory responsibilities. Education & Experience: Associate degree in Life Science or related field with two or more years of laboratory experience, preferred Two or more years of experience in a commercial food-testing or analytical laboratory Or equivalent combination of education and experience Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures Broad knowledge of concepts, practices, and procedures of a food testing laboratory Ability to travel when necessary Physical Demands/Work Environment: Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens Noise level varies from quiet to loud Temperature varies from hot to cold Interactive and fast-paced team oriented tasks Overnight Travel is required at the discretion of management Occasionally lift and/or move up to 25 pounds Color vision and depth perception Benefits: Progressive 401k Retirement Savings Plan Employer Paid Short- Term and Long-Term Disability, and Life Insurance Group Medical Tuition Reimbursement Flexible Spending Accounts Dental Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status. Tuesday - Saturday 9pm-5:30am